A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924041



Internal ID22699268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66476213..66588523hg38UCSC Ensembl
chr7:65941200..66053510hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38112311
hg19112311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1897n209
Supporting Variantsnssv17441033
Samples
Known GenesLOC493754
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924041
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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